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Completed Phase 3 Interventional Results available

Study to Assess the Efficacy and Safety of Ruxolitinib in Patients With COVID-19 Associated Cytokine Storm

ClinicalTrials.gov ID: NCT04362137

Public ClinicalTrials.gov record NCT04362137. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 6:05 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 3 Randomized, Double-blind, Placebo-controlled Multi-center Study to Assess the Efficacy and Safety of Ruxolitinib in Patients With COVID-19 Associated Cytokine Storm (RUXCOVID)

Study identification

NCT ID
NCT04362137
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
432 participants

Conditions and interventions

Interventions

  • Ruxolitinib Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 1, 2020
Primary completion
Oct 16, 2020
Completion
Oct 16, 2020
Last update posted
Oct 10, 2021

2020

United States locations

U.S. sites
11
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Novartis Investigative Site Fullerton California 92835
Novartis Investigative Site Aurora Colorado 80045
Novartis Investigative Site Denver Colorado 80205
Novartis Investigative Site Atlanta Georgia 30312
Novartis Investigative Site Idaho Falls Idaho 83404
Novartis Investigative Site Ann Arbor Michigan 48109
Novartis Investigative Site Newark New Jersey 07103
Novartis Investigative Site The Bronx New York 10461
Novartis Investigative Site Mesquite Texas 75149
Novartis Investigative Site Seattle Washington 98104
Novartis Investigative Site Madison Wisconsin 53705-3611

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 50 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04362137, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 10, 2021 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04362137 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →